Monitoring disease activity and treatment response in ankylosing spondylitis: a retrospective study of hematologic inflammatory markers.

IF 3.2 3区 医学 Q2 RHEUMATOLOGY Rheumatology International Pub Date : 2024-12-28 DOI:10.1007/s00296-024-05763-6
Oznur Sadioglu Cagdas, Neslihan Gokcen, Ayten Yazici, Ayse Cefle
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Abstract

Background: Hematological markers such as the neutrophil-lymphocyte ratio (NLR), monocyte-lymphocyte ratio (MLR), and platelet-lymphocyte ratio (PLR) are reliable indicators of inflammation. This study aims to investigate the potential role of these markers in assessing disease activity and treatment response in biologic-naive Ankylosing Spondylitis (AS) patients following the initiation of biological agents.

Materials and methods: We designed this study as a retrospective cohort study with data obtained from a single center. The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and The Bath Ankylosing Spondylitis Functional Index (BASFI) were used to evaluate disease activity and functional status of AS patients. Laboratory results at baseline, 3rd, 6th, and 12th months were documented. We calculated hematologic inflammatory markers for each visit. Mean platelet volume (MPV) and red cell distribution width (RDW) were also noted.

Results: 54 biologic-naive patients with AS were included in this study. These inflammatory markers, except RDW, decreased over time. BASDAI, BASFI, CRP and ESR were significantly lower at 3rd, 6th, and 12th months compared to baseline values (all p < 0.001). Furthermore, NLR, PLR, and MLR showed a statistically significant decrease at 3rd, 6th, and 12th months compared to baseline values (all p < 0.001). However, when comparing the values at the 3rd, 6th, and 12th months, no statistically significant differences were observed. We also found no correlation between hematological inflammatory markers and BASDAI scores, despite observing some correlations between hematological markers and acute phase reactants.

Conclusion: These markers could be valuable assessment tools for indicating disease activity and monitoring patients with AS after initiating biological treatment.

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监测强直性脊柱炎的疾病活动和治疗反应:血液学炎症标志物的回顾性研究。
背景:血液学指标如中性粒细胞-淋巴细胞比率(NLR)、单核细胞-淋巴细胞比率(MLR)和血小板-淋巴细胞比率(PLR)是炎症的可靠指标。本研究旨在探讨这些标志物在生物初始强直性脊柱炎(AS)患者开始使用生物制剂后评估疾病活动性和治疗反应中的潜在作用。材料和方法:我们将本研究设计为回顾性队列研究,数据来自单一中心。采用Bath强直性脊柱炎疾病活动性指数(BASDAI)和Bath强直性脊柱炎功能指数(BASFI)评价AS患者的疾病活动性和功能状态。记录基线、第3、第6和第12个月的实验室结果。我们计算了每次就诊的血液学炎症标志物。平均血小板体积(MPV)和红细胞分布宽度(RDW)也被记录。结果:54例AS生物初治患者纳入本研究。除了RDW外,这些炎症标志物随着时间的推移而降低。与基线值相比,BASDAI、BASFI、CRP和ESR在第3、6和12个月时显著降低(均为p)。结论:这些标志物可以作为指示疾病活动性和开始生物治疗后监测AS患者的有价值的评估工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Rheumatology International
Rheumatology International 医学-风湿病学
CiteScore
7.30
自引率
5.00%
发文量
191
审稿时长
16. months
期刊介绍: RHEUMATOLOGY INTERNATIONAL is an independent journal reflecting world-wide progress in the research, diagnosis and treatment of the various rheumatic diseases. It is designed to serve researchers and clinicians in the field of rheumatology. RHEUMATOLOGY INTERNATIONAL will cover all modern trends in clinical research as well as in the management of rheumatic diseases. Special emphasis will be given to public health issues related to rheumatic diseases, applying rheumatology research to clinical practice, epidemiology of rheumatic diseases, diagnostic tests for rheumatic diseases, patient reported outcomes (PROs) in rheumatology and evidence on education of rheumatology. Contributions to these topics will appear in the form of original publications, short communications, editorials, and reviews. "Letters to the editor" will be welcome as an enhancement to discussion. Basic science research, including in vitro or animal studies, is discouraged to submit, as we will only review studies on humans with an epidemological or clinical perspective. Case reports without a proper review of the literatura (Case-based Reviews) will not be published. Every effort will be made to ensure speed of publication while maintaining a high standard of contents and production. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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